A mum is living with the awful uncertainty of not knowing what tumour type her teenage daughter has despite several surgeries, ongoing treatment and two recurrences.

Laura Hobbs lost her 72-year-old dad to an aggressive brain tumour just 25 days after having symptoms the family originally thought were a reaction to the Covid vaccination.

A wife who lost her husband to a brain tumour has praised our website for being her ‘go-to’ place for all the information she needed following his shock diagnosis.

A loving wife spent 11 years managing symptoms of an undiagnosed brain tumour whilst she cared for her unwell mother and her husband who also had cancer.

The Brain Tumour Charity is continuing its partnership with ethical, sustainable clothing brand Teemill to launch a brand new range of clothes under its well-known ‘A Cure Can’t Wait’ slogan.

A student who was diagnosed with a brain tumour when he was studying at university has praised The Brain Tumour Charity’s support and information for getting him through his ordeal.

Research funded by The Brain Tumour Charity has revealed a new way of classifying meningiomas that can more accurately predict how a tumour will behave and help clinicians identify patients who may benefit from more aggressive treatment earlier. Crucially, researchers have also potentially identified the first-ever drug treatment for most-aggressive forms of meningioma.

A mum-of-two who was diagnosed with a brain tumour after a holiday in Las Vegas and its recurrence when she was pregnant is fundraising for The Brain Tumour Charity.

A family who lost their dad and husband to an aggressive brain tumour just days after diagnosis has shared how his influence lives on through his ‘life lessons’.

Andrew and Julie Elsworth’s Twilight Walk on Sunday 3 was especially poignant because Andrew’s only son, and Julie’s stepson, Daniel, passed away only two weeks ago, aged just 35.

Add your voice to ours by signing the Parliamentary Petition calling for the Government to urgently invest in establishing the UK as a world-beating force in cancer survival and care.

A mum who had been to the GP countless times with excruciating headaches was only diagnosed with a brain tumour after a full body scan following her pancreatic tumour diagnosis.

Keen to help others, Millie has shared advice and tips for other young people, who may be growing up with a parent who has a brain tumour diagnosis.

An adventurer who was diagnosed with a brain tumour after first experiencing symptoms whilst climbing a volcano is taking on a mountaineering challenge to fundraise for The Brain Tumour Charity.

A travel addict who lives with the ongoing effects of a brain tumour which hemorrhaged when she was a teenager hasn’t let it stop her from enjoying life today.

A mum-of-two who was diagnosed with an aggressive brain tumour seven years ago is crediting a positive mental attitude to helping her to navigate daily life alongside the condition.

A woman who was diagnosed with a brain tumour less than two years after losing her mum to the disease is encouraging others to live life by seizing the day.

A successful lawyer credits children’s literature for helping her to rediscover a love of reading after her brain tumour diagnosis and treatment left her with severe fatigue and reduced concentration.

Our Optical Engagement Manager, Lorcan Butler, is delighted to be partnering with opticians and optometrists in Scotland to help diagnose brain tumours earlier.

A pregnant mum-of-three, who feared that she would never see the face of her unborn son as a brain tumour was crushing her optic nerve, is fundraising to find a cure for the disease.

Modern molecular profiling of medulloblastomas recently highlighted a previously unrecognised treatment benefit in a major international clinical trial.

A family spent the pandemic making memories with their four-year-old son who lost his life just a few months later to one of the most aggressive brain tumours his doctors had ever seen.

Our supporters, fundraisers and partners are a truly inspirational bunch! From the corporate world to comedy and more, read about just some of the ways our community are raising funds and awareness – as well as challenging themselves to go further, faster for a cure.

Rhudi Baume-Kennedy, 20, explains how his experience of spending nine months trying to get a diagnosis for his symptoms has driven his support for The Charity’s work.